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胎儿弯曲杆菌TK菌株中S层的缺失是由sapA同源簇中的一个缺失所致。

A deletion in the sapA homologue cluster is responsible for the loss of the S-layer in Campylobacter fetus strain TK.

作者信息

Fujita M, Moriya T, Fujimoto S, Hara N, Amako K

机构信息

Department of Bacteriology, Faculty of Medicine, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-82, Japan.

出版信息

Arch Microbiol. 1997 Apr;167(4):196-201. doi: 10.1007/s002030050435.

Abstract

The surface array protein (SAP) of Campylobacter fetus strain TK is encoded by seven homologous sapA genes clustered on the chromosomal DNA. The spontaneously arising variant strain TK(SAP-) produces no SAP and carries an approximately 10-kb chromosomal deletion. To elucidate the mechanism underlying the loss of SAP synthesis, we analyzed the region containing the sapA homologues and the deletion. We constructed a physical map of the sapA cluster region by aligning the clones that contain sapA homologues. These analyses demonstrated that all sapA homologues were located within a limited region of about 50 kb of chromosomal DNA of strain TK. The TK(SAP-) deletion was located within this cluster and was 13.3 kb in size. The deletion occurred between two sapA homologues and resulted in the formation of a chimeric sapA homologue in the variant strain. Sequence analysis of the upstream regions and the conserved regions of all sapA homologues revealed a high degree of similarity. However, only one sapA homologue contained a putative promoter sequence. This promoter sequence was located in the deleted region. Thus, the deletion of the promoter appears to be responsible for the loss of SAP expression in TK(SAP-).

摘要

胎儿弯曲杆菌TK菌株的表面阵列蛋白(SAP)由聚集在染色体DNA上的7个同源sapA基因编码。自发产生的变异菌株TK(SAP-)不产生SAP,并携带约10 kb的染色体缺失。为了阐明SAP合成缺失的潜在机制,我们分析了包含sapA同源物的区域和缺失情况。我们通过比对包含sapA同源物的克隆构建了sapA簇区域的物理图谱。这些分析表明,所有sapA同源物都位于菌株TK约50 kb的染色体DNA有限区域内。TK(SAP-)缺失位于该簇内,大小为13.3 kb。缺失发生在两个sapA同源物之间,导致变异菌株中形成嵌合的sapA同源物。对所有sapA同源物的上游区域和保守区域的序列分析显示出高度相似性。然而,只有一个sapA同源物包含推定的启动子序列。该启动子序列位于缺失区域。因此,启动子的缺失似乎是TK(SAP-)中SAP表达缺失的原因。

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